Medical Monitor / Study Physician (Home Based)

About the role

Parexel is seeking an experienced Study Physician to work remotely for a key sponsor in the EMEA region. You will be medically responsible for clinical trials from design through reporting, ensuring high‑quality medical oversight throughout.

Key responsibilities

• Prepare and maintain high‑quality clinical trial protocols, minimizing amendments.
• Provide medical expertise from trial design to final clinical trial report.
• Integrate medically relevant data and risks into quality and risk‑management plans.
• Co‑author Clinical Quality Monitoring plans and conduct ongoing medical data reviews.
• Support risk‑based quality management and ensure compliance with ICH‑GCP.

Required profile

• Physician (MD) with a medical thesis and at least 4 years of active clinical practice.
• Specialisation in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology or Emergency Medicine is highly desirable.
• Experience in pharma or CRO environments, preferably in medical monitoring, project management or pharmacovigilance.
• Strong understanding of ICH‑GCP and relevant regulatory guidance.
• Previous experience as a medical monitor and familiarity with data visualization or IT systems is a plus.

Required skills

• ICH‑GCP knowledge
• Data visualization systems
• IT systems for clinical development